chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105203612105203613GT19GENIChomozygous125831015
3105203630105203631CG19GENIChomozygous125831017
3105204157105204158TC10GENIChomozygous111993345
3105204281105204282CT13GENIChomozygous111993347
3105204325105204326GA18GENIChomozygous111993349
3105204466105204467GA9GENIChomozygous111993351
3105205088105205089GA24GENIChomozygous111993353
3105205258105205259CT21GENIChomozygous111993355
3105205269105205270CG12GENICheterozygous111993357
3105205377105205378AG25GENIChomozygous111993359
3105205482105205483TA25GENIChomozygous111993361
3105205841105205842AG13GENIChomozygous111993363
3105206138105206139AT20GENICpossibly homozygous111993365
3105210968105210969CT19GENIChomozygous111993369
3105214606105214607TA15GENIChomozygous111993371